VISTAPHARM FDA Approval ANDA 211063

ANDA 211063

VISTAPHARM

FDA Drug Application

Application #211063

Application Sponsors

ANDA 211063VISTAPHARM

Marketing Status

Prescription001
Prescription002

Application Products

001TABLET;ORAL25MG0CHLORTHALIDONECHLORTHALIDONE
002TABLET;ORAL50MG0CHLORTHALIDONECHLORTHALIDONE

FDA Submissions

UNKNOWN; ORIG1AP2019-02-26STANDARD

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAB
002PrescriptionAB

CDER Filings

VISTAPHARM
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 211063
            [companyName] => VISTAPHARM
            [docInserts] => ["",""]
            [products] => [{"drugName":"CHLORTHALIDONE","activeIngredients":"CHLORTHALIDONE","strength":"25MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"},{"drugName":"CHLORTHALIDONE","activeIngredients":"CHLORTHALIDONE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"02\/26\/2019","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2019-02-26
        )

)

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